Proteomic profiling of exudates from diabetic foot ulcers and acute

139 Pages·2013·6.57 MB·English

by  Krisp, Christopph

Proteomic profiling of exudates from diabetic
foot ulcers and acute wounds using mass
spectrometry

Christoph Krisp

Bachelor of Chemistry, Ruhr University Bochum
Master of Chemistry, Ruhr University Bochum

A thesis presented for the degree of
Doctor rerum naturalium
Dr. rer. nat.

Ruhr University Bochum Macquarie University
Faculty of Chemistry and Biochemistry Faculty of Science
Department of Analytical Chemistry Department of Chemistry and
Biomolecular Sciences

May 2013
Declaration
The work presented in this thesis titled “Proteomic profiling of exudates from diabetic
foot ulcers and acute wounds using mass spectrometry” has not been submitted for a higher
degree to any other university or institution other than Macquarie University, Sydney,
Australia and Ruhr University Bochum, Bochum, Germany under the Cotutelle
Agreement.
Acknowledgement
First of all I would like to thank my two magnificent supervisors Mark Molloy and
Dirk Wolters.
Dirk, you gave me the opportunity to develop into an independent and self-confident
scientist, able to assume responsibility for myself and critically reflect upon the work I am
doing. You gave me the space I needed to accomplish my work and challenge myself, but
were around when I needed your help. I acknowledge your advisedly allocation of
additional projects, which taught me to think outside of the box and be open-minded for
new ideas.
Mark, I would like to thank you for the fantastic time I had working with your group.
You are calm, thoughtful, focused and well organized. The way you supervised me let me
transcend my own boundaries which made me succeed in ways I had never dreamed of.
You have a special way to motivate people with perfect timing. Your motivation always
reached me when I needed it most. You were the person who proposed the Cotutelle
program to me and who believed in me to get chosen for this program. For that I will
always be deeply grateful. The time with your group increased my passion for science and
made me to the scientist I am today. Thank you.

Further, I would like to thank Matthew McKay for the knowledge and expertise he
shared with me and the support he gave me during all the challenges I came across.
Matthew you helped me keep my patience with the instruments and taught me fundamental
skills. I appreciate the thrust you put in me.
This continues with my gratitude to past and present students and staffs at Macquarie
University, APAF, and Ruhr University Bochum, especially my colleagues and friends at
the Molloy work group, the biomarker discovery Laboratory, and the Wolters work group.
You made my PhD studies a memorable time in my life.

I want to express my thanks to Ruhr University Bochum and Macquarie University to
allow me to conduct my studies under a joint project acknowledged by both universities.
The Cotutelle program is a wonderful program that not only gave me the opportunity to
expand my expertise in my research field, but in my whole life. Only because of this
program I was able to get to know many wonderful people who became an important part
of my life. Further, I would like to thank Macquarie University for granting me a
Macquarie University Research Excellence Scholarships (MQRES) to support me while I
worked at Macquarie University.

I thank the laboratory for Molecular Oncology and Wound Repair located in the
department of Plastic Surgery at the Ruhr University Hospital “Bergmansheil” especially
Lars Steinsträßer and Frank Jacobsen for liberally providing the wound fluids.
Further, I want to acknowledge BBraun Melsungen AG in particular Andreas Gmerek
for supporting the haemodialysis work and Luciano Pedrini at the Nephrology and Dialysis
Units at the Bolognini Hospital in Italy who provided the haemodialysis samples.

Finally my thanks go to my family and friends around the world who have always
been supportive und sympathetic particularly in busy times. You helped me maintain my
work-life balance and made every moment enjoyable.
I am eminently grateful to have such wonderful and loving parents who were always
there for me and made me to the person I am today. I love you.
Therefore, I would like to address some words in German to you

Liebe Eltern, ich danke Euch für Eure immerwährende Unterstützung die ihr mir über
all die Jahre gegeben habt und dafür, dass ihr immer für mich da gewesen seid und auch
weiterhin für mich da seid werdet. Ohne Eure Motivation hätte ich es niemals soweit
geschafft. Ihr habt mir gezeigt, was im Leben wichtig ist und dass man für seine
Überzeugungen einstehen soll. Ihr habt mich zu dem Menschen gemacht, der ich heute bin.
Mit Eurer liebenswerten und fürsorglichen Art habt ihr mir ein Zuhause geboten, das sich
jeder nur wünschen kann. Für all dies und noch viel, viel mehr möchte ich mich bei Euch
bedanken. Ich habe Euch lieb.
Parts of this work have been published or are submitted for publication in scientific
journals.

[1] Christoph Krisp; Caroline Kubutat; Andreas Kyas; Lars Steinsträßer; Frank Jacobsen;
Dirk A. Wolters, Boric acid gel enrichment of glycosylated proteins in human wound
fluids. Journal of Proteomics 2010, 74, (4), 502-509.
[2] Christoph Krisp; Matthew J McKay; Dirk A. Wolters; Mark P. Molloy,
Multidimensional protein identification technology-selected reaction monitoring improving
detection and quantification for protein biomarker studies. Analytical Chemistry 2012, 84,
(3), 1592-1600.
*This manuscript was selected by the faculty of thousand as one of the top 2% of published
articles in biology and medicine*
*Further this manuscript was awarded by Macquarie University, Faculty of Science with
the Biomolecular Frontiers Research Postgraduate Prize for the best internationally peer-
reviewed paper by a postgraduate student as first author accepted for publication*
[3] Christoph Krisp; Frank Jacobsen; Lars Steinsträßer; Matthew J McKay; Mark P
Molloy; and Dirk A. Wolters, Proteome analysis reveals anti-angiogenic environments in
chronic wounds of diabetes mellitus type 2 patients, Proteomics under revision

Publications achieved during the period of the doctoral studies which are not included in
this thesis.

[4] Lars Steinsträßer; Frank Jacobsen; Tobias Hirsch; Marco Kesting; Caroline Chojnacki;
Christoph Krisp; Dirk A. Wolters, Immunodepletion of high-abundant proteins from acute
and chronic wound fluids to elucidate low-abundant regulators in wound healing. BMC
Research Notes 2010, 3, (1), 335.
[5] Christoph Krisp; Sarah A. Randall; Matthew J. McKay; Mark P. Molloy, Towards
clinical applications of selected reaction monitoring for plasma protein biomarker studies.
Proteomics – Clinical Applications 2011, 6, (1-2), 42-59.
[6] Peter Lüdike; Ulrike B. Hendgen-Cotta; Julia Sobierajski; Matthias Totzeck; Marcel
Reeh; Manfred Dewor; Hongqi Lue; Christoph Krisp; Dirk A. Wolters; Malte Kelm;
Jürgen Bernhagen, Tienush Rassaf, Cardioprotection Through S-Nitros(yl)ation of
Macrophage Migration Inhibitory Factor. Circulation 2012, 125, (15), 1880-1889.
[7] Miriam M. Cortese-Krott; Ana Rodriguez-Mateos; Roberto Sansone; Gunter G. C.
Kuhnle; Sivatharsini Thasian-Sivarajah; Thomas Krenz; Patrik Horn; Christoph Krisp;
Dirk A. Wolters; Christian Heiß; Klaus-Dietrich Kröncke; Neil Hogg; Martin Feelisch;
Malte Kelm, Human red blood cells at work: identification and visualization of
erythrocytic eNOS activity in health and disease, Blood 2012, 120, (20), 4229-4237.
[8] Jessica Jacob; Christina Marx; Vera Kock; Olga Reifschneider; Benjamin Fränzel;
Christoph Krisp; Dirk A. Wolters; Ulrich Kück, Identification of a Chloroplast
Ribonucleoprotein Complex Containing Trans-splicing Factors, Intron RNA and Novel
Components, Molecular and Cellular Proteomics accepted for publication

Additionally, parts of this were presented as posters at international scientific conferences

[1] Christoph Krisp; Dirk A. Wolters. Immunodepletion of human wound fluids - always
the best way to go? 9th annual meeting of the Human Protein Organization (HUPO), 2010,
Sydney, Australia.
[2] Christoph Krisp; Matthew J. McKay; Dirk A. Woltetrs; Mark P. Molloy, From
SHOTGUN to SNIPER – Proteomic analysis of human wound fluids. 16th Proteomics
symposium of the Austalasian Proteomics Society (APS), 2011, Lorne, Australia.
[3] Christoph Krisp; Matthew J. McKay; Dirk A. Woltetrs; Mark P. Molloy, From
SHOTGUN to SNIPER – Pipeline for discovery and validation of human wound fluid
biomarkers. 59th annual meeting of the American Society of Mass Spectrometry (ASMS),
2011 Denver, Colorado, USA
[4] Christoph Krisp; Andreas Gmerek; Jürgen Wagner; Dirk A. Wolters, The Way to In-
Vivo cut-off Profiles: Protein Removal Efficiency of two different haemodialysis
membranes using MudPIT-Analysis. 48th annual meeting of the European Renal
Association - European Dialysis and Transplant Association (ERA-EDTA), 2011, Prague,
Czech Republic.
[5] Christoph Krisp; Matthew J. McKay; Dirk A. Woltetrs; Mark P. Molloy, MudPIT-SRM
– a highly multiplexed strategy for low abundant protein biomarker identification. 10th
annual meeting of HUPO, 2011, Geneva, Switzerland.
[6] Christoph Krisp; Matthew J. McKay; Mark P. Molloy; Dirk A. Woltetrs, Proteome
Analysis of Human Wound Fluids - MudPIT-FTMS and MudPIT-SRM as strategies of
choice for reliable Biomarker identification and validation. 60th annual meeting of ASMS,
2012, Vancouver, Canada.
[7] Christoph Krisp; Andreas Gmerek; Jürgen Wagner; Dirk A. Wolters, MudPIT analysis
as a proteomic tool for novel potential uremic toxin identification in haemodialysis filtrates
49th annual meeting of ERA-EDTA, 2012, Paris, France.

The biomarker discovery study of human wound fluids of patients with chronic foot ulcers
(Chapter 5), the study of proteins in spent dialysates to estimate the elimination efficiency
of dialysis membranes applied to chronic heamodialysis patients (Chapter 8), and the
development of a glycoprotein enrichment strategy using a boric acid derivate (Chapter 4)
were conducted at the bio molecular mass spectrometry work group of Dr. Dirk Wolters
located in the Faculty of Chemistry and Biochemistry, Department of Analytical Chemistry
at the Ruhr University Bochum, Bochum, Germany.

The SRM validation of identified regulation differences of proteins in human wound fluids
(Chapter 6), and the development of the MudPIT-SRM strategy for improved bio marker
detection (Chapter 7) were carried out at the work group of Associate Professor Mark
Molloy located in the Faculty of Science, Department of Chemistry and Biomolecular
Sciences at Macquarie University, Sydney, Australia.
Awards
Macquarie University Research Scholarship (MQRES)

Macquarie University Postgraduate Research Fund (PGRF), June 2011

Macquarie University Faculty of Science Biomolecular Frontiers Research Postgraduate
Prize
Awarded for the best internationally peer-reviewed paper by a postgraduate student as first
author accepted for publication
Abstract
Poor healing, chronic wounds at the lower extremities of diabetes mellitus patients are
a debilitating condition. . Numerous studies have revealed dramatic differences in several
repair regulation steps with these chronic wounds, but additional information is needed to
understand the role of specific proteins in these processes.
In this study, mass spectrometry (MS) was employed to investigate proteins in
exudates from type 2 diabetes mellitus foot ulcers and they were compared to proteins
found in acute wound exudates of burn victims that were otherwise healthy.
Initial experiments were conducted to investigate strategies to reduce sample
complexity using high abundant protein depletion or post-translational modification based
enrichments. High abundant protein depletion was proven to be not applicable to the
exudates, as MS investigation revealed substantial co-elimination of important proteins
involved in healing processes. The enrichment of glycosylated proteins was demonstrated
but found to be unsuitable for large-scale comparative studies as needed for wound
exudates. Therefore, liquid-chromatography-tandem mass spectrometry (LC-MS/MS) was
performed on undepleted and unenriched wound exudates.
Multi-dimensional protein identification technology-MS/MS (MudPIT-MS/MS) using
high resolution MS of 10 chronic and 6 acute wounds revealed expression level differences
of proteins in inflammation signalling, predominately S100 proteins, impairment of pro-
and anti-inflammatory signalling, elevated matrix metalloproteinase (MMP) activity, anti-
angiogenic environment, and elevated cell death with apoptotic and necrotic motifs. The
expression level differences of selected proteins were confirmed by selected reaction
monitoring (SRM) conducted on 9 chronic and 9 acute wounds. Further, S100A8 and
S100A9 elevation was confirmed by western blot. The enzyme activity of MMP2 and
MMP9 were investigated with gelatin zymography, confirming higher MMP2expression in
chronic wounds.
A novel MudPIT-SRM workflow was developed to enable the SRM validation study.
The combination of high resolving liquid chromatography with highly sensitive SRM
demonstrated significant detection improvement (90%) in peptide quantitation on human
plasma proteins and human wound fluids. In addition to the analysis of wound exudates,
the membrane dependent protein elimination efficiency of two high-flux haemodialysis
filters was investigated. Within a sample cohort of 9 chronic haemodialysis patients, better
uremic toxin elimination by Xevonta Hi23 membrane (Amembrix® filter devices) were
identified in comparison to Polyflux 210H (Gambro PolyamixTM).
In summary this thesis has revealed new insight into specific proteins regulating
chronic wounds in diabetes mellitus patients, developed a novel MS workflow by
combining MudPIT with SRM and determined the optimum haemodialysis filter to
eliminate uremic toxins.